Canonical Allele Identifier: PA2828090680
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val339Ile
CA276776626
NM_001363528.2:c.1015G>A